Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g46260 A09 51088382 C T synonymous_variant LOW c.6006G>A|p.Lys2002Lys S238
2 BAA09g46260 A09 51088526 G A synonymous_variant LOW c.5950C>T|p.Leu1984Leu S150
3 BAA09g46260 A09 51088852 G A missense_variant MODERATE c.5761C>T|p.Arg1921Cys S59
4 BAA09g46260 A09 51089457 G A missense_variant MODERATE c.5524C>T|p.His1842Tyr S190
5 BAA09g46260 A09 51089630 G A missense_variant MODERATE c.5351C>T|p.Ala1784Val S305
6 BAA09g46260 A09 51091824 C T synonymous_variant LOW c.3939G>A|p.Leu1313Leu S67
7 BAA09g46260 A09 51091888 C T missense_variant MODERATE c.3875G>A|p.Arg1292Lys S68
8 BAA09g46260 A09 51092381 C T missense_variant MODERATE c.3571G>A|p.Gly1191Arg S250
9 BAA09g46260 A09 51093262 G A missense_variant MODERATE c.2885C>T|p.Pro962Leu S288
10 BAA09g46260 A09 51094035 C T intron_variant MODIFIER c.2368-190G>A| S199
11 BAA09g46260 A09 51094493 G A synonymous_variant LOW c.2253C>T|p.Phe751Phe S274
12 BAA09g46260 A09 51094595 G A intron_variant MODIFIER c.2194-43C>T| S165
13 BAA09g46260 A09 51095160 C T synonymous_variant LOW c.1878G>A|p.Gln626Gln S151
S166
S167
S263
14 BAA09g46260 A09 51095240 C T missense_variant MODERATE c.1798G>A|p.Asp600Asn S267
15 BAA09g46260 A09 51095849 G A missense_variant MODERATE c.1556C>T|p.Ser519Phe S151
S263
16 BAA09g46260 A09 51096525 C T missense_variant MODERATE c.1036G>A|p.Asp346Asn S260
17 BAA09g46260 A09 51098603 C T missense_variant MODERATE c.289G>A|p.Gly97Arg S191
18 BAA09g46260 A09 51098962 G A intron_variant MODIFIER c.151-221C>T| S8
19 BAA09g46260 A09 51099263 C T intron_variant MODIFIER c.150+274G>A| S30
S31
20 BAA09g46260 A09 51099455 C T intron_variant MODIFIER c.150+82G>A| S87
21 BAA09g46260 A09 51100528 G A upstream_gene_variant MODIFIER c.-714C>T| S274
22 BAA09g46260 A09 51101544 G A upstream_gene_variant MODIFIER c.-1730C>T| S247
23 BAA09g46260 A09 51101703 C T upstream_gene_variant MODIFIER c.-1889G>A| S286
24 BAA09g46260 A09 51101881 G A upstream_gene_variant MODIFIER c.-2067C>T| S72